Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs121918075
TTR
0.752 0.280 18 31598632 missense variant A/G snv 15
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs12041331 0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs28939068 0.790 0.200 20 23635330 missense variant A/T snv 9
rs1035071612 0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 9
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv 8
rs5050
AGT
0.827 0.200 1 230714140 intron variant T/C;G snv 7
rs12566888 0.807 0.280 1 156899255 intron variant G/T snv 0.26 7
rs1394871591 0.827 0.200 9 104903619 missense variant G/C snv 4.8E-06 5
rs79524815 0.851 0.240 7 18658708 intron variant T/G snv 3.8E-02 4
rs1861493 0.851 0.280 12 68157416 intron variant G/A snv 0.76 4
rs2229634 0.851 0.240 6 33670403 synonymous variant C/A;T snv 4.0E-06; 0.33 4
rs34487851 0.882 0.200 2 106026098 regulatory region variant A/G snv 0.28 3
rs899162 0.882 0.160 5 135459219 downstream gene variant G/A snv 1.0E-01 3
rs1297968881
APP
0.882 0.200 21 26112137 missense variant C/T snv 4.0E-06 3
rs63750973
APP
0.882 0.120 21 25891792 missense variant G/A snv 3
rs7849782 0.925 0.160 9 101664982 intron variant C/A;G;T snv 3
rs16921209 0.882 0.160 10 20879174 intron variant C/G snv 4.6E-02 3
rs7637803 0.882 0.160 3 151371438 intron variant C/G;T snv 3
rs28834970 0.882 0.120 8 27337604 intron variant T/C snv 0.32 3
rs17076896 0.882 0.160 13 19181923 upstream gene variant T/C snv 8.3E-02 3
rs9309308 0.925 0.160 2 24771701 downstream gene variant T/C snv 0.18 2